Items where Author is "Mirfakhraie, R."

Article

(2024) Identification of novel mutations in TPK1 and SLC19A3 genes in families exhibiting thiamine metabolism dysfunction syndrome. Heliyon. p. 7.

(2024) National and subnational burden of mental disorders in Iran (1990-2019): findings of the Global Burden of Disease 2019 study. Lancet Global Health. E1984-E1992. ISSN 2214-109X

(2023) Burden of tracheal, bronchus, and lung cancer in North Africa and Middle East countries, 1990 to 2019: Results from the GBD study 2019. Frontiers in Oncology. ISSN 2234943X (ISSN)

(2021) Targeted sequencing of CDH23 and GJB2 genes in an Iranian pedigree with Usher syndrome and non-syndromic hearing loss. Gene Reports.

(2021) Whole exome sequencing identified a novel homozygous ARV1 mutation in an Iranian family with developmental and epileptic encephalopathy-38. META GENE. ISSN 2214-5400 J9 - META GENE

(2017) Evaluation of promoter methylation status of MLH1 gene in Iranian patients with colorectal tumors and adenoma polyps. Gastroenterology and hepatology from bed to bench. S117-S121. ISSN 2008-2258 (Print) 2008-2258 (Linking)